HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Chloromethyl)-1,3-thiazole → HCID 57974282, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Chloromethyl)-1,3-thiazole | HCID 14090864 | — |
| Reactant | HCID 69056760 | HCID 69056760 | — |
| Product | HCID 57974282 | HCID 57974282 | 31% |
Reaction Steps
The procedure described in Example 3 was repeated using 2-(chloromethyl)-1,3-thiazole and 2-hydroxy-N-[(2R)-2-({4-[(4-hydroxy-3-methylphenyl)amino]quinazolin-5-yl}oxy)propyl]acetamide (obtained as described in Example 82, preparation of starting materials) to give the title compound as a light brown solid in 31% yield; NMR spectrum (DMSO-d6) 1.39 (d, 3H), 2.25 (s, 3H), 3.42 (dt, 1H), 3.73 (m, 1H), 3.79 (d, 2H), 4.94 (m, 1H), 5.44 (s, 2H), 5.47 (t, 1H), 7.09 (d, 1H), 7.23 (d, 1H), 7.30 (d, 1H), 7.58 (d, 1H), 7.63 (dd, 1H), 7.69 (t, 1H), 7.77 (d, 1H), 7.84 (d, 1H), 8.16 (t, 1H), 8.43 (s, 1H), 9.96 (s, 1H); Mass spectrum MH+ 480.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07625908B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-7d87caf7e0a04fa986f21712fafefaac |
| Source note | uspto-grants-2009_12 |