HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295640Generated: October 30, 2026
Thionyl Chloride → 6-[4-(Chloromethyl)phenyl]-N-((R)-1-phenylethyl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine
https://huagongshe.com/reaction/1295640
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 59756755 | HCID 59756755 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 6-[4-(Chloromethyl)phenyl]-N-((R)-1-phenylethyl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine | HCID 59756711 | — |
Reaction Steps
A solution of thionyl chloride (25.7 ml, 0.328 mol) in 180 ml of toluene is cooled to −10° C. Solid {4-[4-((R)-1-phenyl-ethylamino)-7H-pyrrolo[2,3-d]pyrimidin-6-yl]-phenyl}-methanol (11.3 g, 0.0328 mol) is added in 8 portions over a range of 1 h. The temperature is then increased slowly to 0° C. and the mixture stirred for 2 h. The cold reaction mixture is filtered and the solid washed with toluene and ether. The crude product is suspended in water and treated with saturated sodium bicarbonate solution until the mixture turns basic. The mixture is stirred well for about 10 min and filtered. The solid is thoroughly washed with water and dried under reduced pressure to give the title compound; m.p. >320° C.; Rf (dichloromethane/ethanol 9:1)=0.46; HPLC tR=10.63 min; MS-ES+: (M+H)+=363.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07244729B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-478d9b67af65484c971a7ec80bf3bf2f |
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| Source note | uspto-grants-2007_07 |
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