2-Pyridinemethanamine → HCID 20374345, compound
Reaction equation
ClC1C=C(C=CC=1)C(Cl)=O.[F:11][S:12]([C:15]1[CH:16]=[C:17]([CH:21]=[CH:22][CH:23]=1)[C:18](Cl)=[O:19])(=[O:14])=[O:13].[NH2:24][CH2:25][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][N:27]=1>>[F:11][S:12]([C:15]1[CH:16]=[C:17]([CH:21]=[CH:22][CH:23]=1)[C:18]([NH:24][CH2:25][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][N:27]=1)=[O:19])(=[O:14])=[O:13]Participants
4
Procedure
Following the procedure of Example 6, Part A, supra., but replacing the 3-chlorobenzoyl chloride as used therein with 6.68 gms. (0.03 mole) of 3-fluorosulfonylbenzoyl chloride and reducing the proportion of 2-aminomethylpyridine as used therein to 3.24 gms. (0.03 mole) there is obtained 3-fluorosulfonyl-N-(2-pyridylmethyl)benzamide in the form of a tan colored solid.
Sources & evidence
- ORD record
- ord-d4dd100f92b7424696a7dd3c32ebe688
- Source dataset
- uspto-grants-1978_01
- Patent number
- US04069224
Reaction notes
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