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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912253Generated: October 31, 2026

Methanesulfonyl chloride → HCID 67385463, compound

https://huagongshe.com/reaction/912253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 67385429HCID 67385429—
ProductHCID 67385463HCID 67385463—

Reaction Steps

In the same manner as Example 1-D-134, using a crude product (80 mg) of 5-{2-morpholin-4-yl-7-[3-(2-piperazin-1-yl-ethyl)-phenyl]-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl}-pyrimidin-2-yl-bis-(4-methoxy-benzyl)-amine obtained in Example 1-D-134 and methanesulfonyl chloride (0.017 ml) instead of acetyl chloride, a crude product of 5-(7-{3-[2-(4-methanesulfonyl-piperazin-1-yl)-ethyl]-phenyl}-2-morpholin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)-pyrimidin-2-yl-bis-(4-methoxy-benzyl)-amine was obtained as a pale yellow solid (82 mg, 93%). Using this crude product (82 mg) of 5-(7-{3-[2-(4-methanesulfonyl-piperazin-1-yl)-ethyl]-phenyl}-2-morpholin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)-pyrimidin-2-yl-bis-(4-methoxy-benzyl)-amine, according to the above Deprotection method 2,5-(7-{3-[2-(4-methanesulfonyl-piperazin-1-yl)-ethyl]-phenyl}-2-morpholin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)-pyrimidin-2-ylamine was obtained as a colorless powder (28 mg, 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022205B2
Source datasetuspto-grants-2011_09
ORD IDord-50a32dee314a402d9171c80f12bf3598
Source noteuspto-grants-2011_09